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NEET CHEMISTRYMedium

Reagents that can be used to convert alcohols to carboxylic acids are: (A) CrO3H2SO4CrO_3 - H_2SO_4 (B) K2Cr2O7+H2SO4K_2Cr_2O_7 + H_2SO_4 (C) KMnO4+KOH/H3O+KMnO_4 + KOH/H_3O^+ (D) Cu,573KCu, 573 K (E) CrO3+(CH3CO)2OCrO_3 + (CH_3CO)_2O

Choose the most appropriate answer from the options given below:

A

(B), (C) and (D) only

B

(B), (D) and (E) only

C

(A), (B) and (C) only

D

(A), (B) and (E) only

Step-by-Step Solution

To convert primary alcohols directly to carboxylic acids, strong oxidising agents are required.

  1. CrO3H2SO4CrO_3 - H_2SO_4 (Jones Reagent): This is a strong oxidising agent that converts primary alcohols to carboxylic acids.
  2. K2Cr2O7+H2SO4K_2Cr_2O_7 + H_2SO_4 (Acidified Potassium Dichromate): A strong oxidising agent commonly used to oxidise alcohols to carboxylic acids.
  3. KMnO4+KOH/H3O+KMnO_4 + KOH/H_3O^+ (Alkaline KMnO4 followed by acid hydrolysis): A very strong oxidising agent that converts primary alcohols to carboxylic acids.
  4. Cu,573KCu, 573 K: This reagent is used for dehydrogenation. It converts primary alcohols to aldehydes and secondary alcohols to ketones, but does not produce carboxylic acids.
  5. CrO3+(CH3CO)2OCrO_3 + (CH_3CO)_2O: This condition is typically used to stop the oxidation of primary alcohols at the aldehyde stage (by forming gem-diacetates), preventing further oxidation to carboxylic acids.

Therefore, only reagents (A), (B), and (C) are suitable for the conversion to carboxylic acids.

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